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New Hydroxyphenylacetic Acids and α-Pyrone Derivative from the Deep-Sea Cold Seep Sediment-Derived Fungus Penicillium corylophilum CS-682.
Zhu, Chi-Sheng; Li, Xiao-Ming; Yang, Sui-Qun; Liu, Yi-Wei; Wang, Bin-Gui; Li, Xin.
Afiliación
  • Zhu CS; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao, 266071, China Tel.
  • Li XM; University of Chinese Academy of Sciences, Yuquan Road 19 A, Beijing, 100049, China.
  • Yang SQ; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao, 266071, China Tel.
  • Liu YW; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao, 266071, China Tel.
  • Wang BG; University of Chinese Academy of Sciences, Yuquan Road 19 A, Beijing, 100049, China.
  • Li X; CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Nanhai Road 7, Qingdao, 266071, China Tel.
Chem Biodivers ; 21(6): e202400584, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38544421
ABSTRACT
Two pairs of new enantiomeric hydroxyphenylacetic acid derivatives, (±)-corylophenols A and B ((±)-1 and (±)-2), a new α-pyrone analogue, corylopyrone A (3), and six andrastin-type meroterpenoids (4-9) were isolated and identified from the deep-sea cold-seep sediment-derived fungus Penicillium corylophilum CS-682. Their structures and stereo configurations were determined by detailed spectroscopic analysis of NMR and MS data, chiral HPLC analysis, J-based configuration analysis, and quantum chemical calculations of ECD, specific rotation, and NMR (with DP4+ probability analysis). Compound 3 showed inhibitory activity against some strains of pathogenic bacteria.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Penicillium / Pironas Idioma: En Revista: Chem Biodivers / Chem. biodivers. (Online) / Chemistry & biodiversity (Online) Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Penicillium / Pironas Idioma: En Revista: Chem Biodivers / Chem. biodivers. (Online) / Chemistry & biodiversity (Online) Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Suiza